rs755287627
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs755287627(A;G) |
| Make rs755287627(G;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 4 |
| Position | 113353494 |
| Gene | ANK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs755287627 |
| dbSNP (classic) | rs755287627 |
| ClinGen | rs755287627 |
| ebi | rs755287627 |
| HLI | rs755287627 |
| Exac | rs755287627 |
| Gnomad | rs755287627 |
| Varsome | rs755287627 |
| LitVar | rs755287627 |
| Map | rs755287627 |
| PheGenI | rs755287627 |
| Biobank | rs755287627 |
| 1000 genomes | rs755287627 |
| hgdp | rs755287627 |
| ensembl | rs755287627 |
| geneview | rs755287627 |
| scholar | rs755287627 |
| rs755287627 | |
| pharmgkb | rs755287627 |
| gwascentral | rs755287627 |
| openSNP | rs755287627 |
| 23andMe | rs755287627 |
| SNPshot | rs755287627 |
| SNPdbe | rs755287627 |
| MSV3d | rs755287627 |
| GWAS Ctlg | rs755287627 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs755287627(G;G) |
| Alt | rs755287627(G;G) |
| Reference | Rs755287627(A;A) |
| Significance | Probable-Pathogenic |
| Disease | Long QT syndrome |
| Variation | info |
| Gene | ANK2 |
| CLNDBN | Long QT syndrome |
| Reversed | 0 |
| HGVS | NC_000004.11:g.114274650A>G |
| CLNSRC | |
| CLNACC | RCV000190219.1, |
